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215587 - Senior Quality Managment Specialist

Industry
PRO
Region
NJ-New Jersey
City
Camden
State
NJ
Rate
Up to $100.00 DOE
Duration
3 months
Description

Chipton-Ross is seeking a Senior Quality Management Specialist for a contract opportunity in Camden, NJ.

BASIC QUALIFICATIONS (REQUIRED SKILLS/EXPERIENCE):

  • Must have working knowledge and experience with AS9100:2016, ISO 9001:2015, and ISO 19011
  • Must be able to assess risk and suggest changes to PEARs
  • Capable of preparing and executing audits of all types and scope
  • Ability to work with all levels and functions within the organization
  • Strong written and verbal communication skills
  • Proficiency in MS Office Suite
  • Familiarity with OASIS and NADCAP databases
  • Strong experience as a SharePoint site admin/owner for document control
  • Experience with eTQ EQMS platform and SAP
  • Quality/purchasing workflows is a plus
  • Must be able to obtain and maintain a DoD Secret Clearance
  • Experience performing internal audits for AS9100 compliance
  • Experience in heavily regulated industries (Aerospace, Space, Medical, Defense)

    • POSITION RESPONSIBILITIES:

  • Lead quality systems coordination, internal audit planning, and QMS document reviews and updates
  • Coordinate migration of QMS documentation to Client Command Media SharePoint site
  • Manage internal audit system and support CAB
  • Perform QMS document control activities including reviews, updates, and releases
  • Maintain corrective action logs and training records
  • Support quality system maintenance and improvement
  • Organize and archive quality records
  • Audit purchasing activities for ASL adherence and supplier quality flowdown
  • Identify internal control issues and ensure root cause analysis and resolution
  • Support MRB and defect tracking as needed
    • Implement procedure review and cross-reference matrix development
  • Track procedure updates and approvals using Excel, SharePoint, and eQMS workflows
  • Manage site training matrix and deliver training as required
  • Ensure QMS and records conform to ISO, DCMA, and other standards
  • Execute internal audits and report findings to leadership
    • Monitor and report quality metrics and trends

    PREFERRED QUALIFICATIONS (DESIRED SKILLS/EXPERIENCE:

  • Lead Auditor Certification
  • Experience with 8D, FMEA, 5-Whys, Pareto analysis
  • Experience calculating CAB metrics and creating charts
  • Certification/training in SharePoint Online O365
  • Experience with nonconformance and corrective action database systems

    • REQUIRED EDUCATION:

  • Accredited Bachelor's degree in a related discipline

    • WORK HOURS:

  • 9/80 work schedule
  • 1st Shift
  • Start time: 7:30–8:00 AM EST


    • Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.

    Contact
    LaVada Pulley
    lpulley@chiptonross.com
    CHIPTON-ROSS, INC.
    420 Culver Boulevard
    Playa Del Rey, CA 90293

    Phone: (310) 414-7800 x260 or (800) 927-9318 x260

    Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.

    Employment will be contingent on candidate clearing pre-employment drug screen and background check.

    Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.